a. The addition of 1 equivalent of bromine at room temperature to the phellandrenes will give three possible di-brominated products. Select either a- or B-phellandrene for this question and draw it in the left box - you can answer this question with either isomer. Draw all three products in the colored boxes depicted - you do not need to depict newly formed stereocenters or show mechanisms. OR a-phellandrene B-phellandrene select either a- or B-phellandrene Br₂ room temperature 3 possible products (see below)

Organic Chemistry
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ISBN:9781305580350
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Chapter10: Alcohols
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**α-phellandrene and β-phellandrene**

**Description:**

α-phellandrene and β-phellandrene are two isomeric diene-containing terpene compounds isolated from eucalyptus plants that are used in fragrances due to their minty and citrusy odors. Use these two compounds to answer the following two questions:

**Question a:**

The addition of 1 equivalent of bromine at room temperature to the phellandrenes will give three possible di-brominated products. Select either α- or β-phellandrene for this question and draw it in the left box – you can answer this question with either isomer. Draw all three products in the colored boxes depicted – you do not need to depict newly formed stereocenters or show mechanisms.

**Diagram:**
- Two molecular structures are shown:
   - α-phellandrene
   - β-phellandrene
   
   (Note: These are chemical structures, with α-phellandrene and β-phellandrene illustrated as hexagonal rings with varying double bonds and substituent methyl groups.)

- Beside these structures:
   - A blank box is labeled "select either α- or β-phellandrene."

- Following the blank box:
   - A reaction arrow labeled "Br₂ / room temperature" points towards three separate blank boxes.

- Under these boxes:
   - The three blank boxes are labeled as "product 1", "product 2", and "product 3" respectively, in blue, red, and gray outlines.

In completing the exercise, students are prompted to select either α- or β-phellandrene, draw the chosen structure in the indicated box, and then predict and depict the three possible di-brominated products in the colored boxes below. Students are not required to show the stereocenters or mechanisms in their drawings.
Transcribed Image Text:**α-phellandrene and β-phellandrene** **Description:** α-phellandrene and β-phellandrene are two isomeric diene-containing terpene compounds isolated from eucalyptus plants that are used in fragrances due to their minty and citrusy odors. Use these two compounds to answer the following two questions: **Question a:** The addition of 1 equivalent of bromine at room temperature to the phellandrenes will give three possible di-brominated products. Select either α- or β-phellandrene for this question and draw it in the left box – you can answer this question with either isomer. Draw all three products in the colored boxes depicted – you do not need to depict newly formed stereocenters or show mechanisms. **Diagram:** - Two molecular structures are shown: - α-phellandrene - β-phellandrene (Note: These are chemical structures, with α-phellandrene and β-phellandrene illustrated as hexagonal rings with varying double bonds and substituent methyl groups.) - Beside these structures: - A blank box is labeled "select either α- or β-phellandrene." - Following the blank box: - A reaction arrow labeled "Br₂ / room temperature" points towards three separate blank boxes. - Under these boxes: - The three blank boxes are labeled as "product 1", "product 2", and "product 3" respectively, in blue, red, and gray outlines. In completing the exercise, students are prompted to select either α- or β-phellandrene, draw the chosen structure in the indicated box, and then predict and depict the three possible di-brominated products in the colored boxes below. Students are not required to show the stereocenters or mechanisms in their drawings.
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